Mechanisms and functions of cellular senescence

被引:976
作者
Herranz, Nicolas [1 ,2 ]
Gil, Jesus [1 ,2 ]
机构
[1] MRC London Inst Med Sci, London, England
[2] Imperial Coll London, Fac Med, Inst Clin Sci, London, England
基金
英国医学研究理事会;
关键词
DNA-DAMAGE-RESPONSE; ONCOGENE-INDUCED SENESCENCE; DEMETHYLASE JMJD3 CONTRIBUTES; SECRETORY PHENOTYPE; BETA-GALACTOSIDASE; IN-VIVO; TUMOR SUPPRESSION; HUMAN FIBROBLASTS; INK4A-ARF LOCUS; POLYCOMB CBX7;
D O I
10.1172/JCI95148
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
100103 [病原生物学]; 100218 [急诊医学];
摘要
Cellular senescence is a highly stable cell cycle arrest that is elicited in response to different stresses. By imposing a growth arrest, senescence limits the replication of old or damaged cells. Besides exiting the cell cycle, senescent cells undergo many other phenotypic alterations such as metabolic reprogramming, chromatin rearrangement, or autophagy modulation. In addition, senescent cells produce and secrete a complex combination of factors, collectively referred as the senescence-associated secretory phenotype, that mediate most of their non-cell-autonomous effects. Because senescent cells influence the outcome of a variety of physiological and pathological processes, including cancer and age-related diseases, pro-senescent and anti-senescent therapies are actively being explored. In this Review, we discuss the mechanisms regulating different aspects of the senescence phenotype and their functional implications. This knowledge is essential to improve the identification and characterization of senescent cells in vivo and will help to develop rational strategies to modulate the senescence program for therapeutic benefit.
引用
收藏
页码:1238 / 1246
页数:9
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